Journal of Southern Medical University ›› 2015, Vol. 35 ›› Issue (06): 848-.
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Abstract: Objective To explore progesterone-induced blocking factor (PIBF) expression in the placenta and blood of patientswith severe preeclampsia and its relationship with immune tolerance imbalance. Methods Forty-seven patients admittedbetween January and December, 2012 were enrolled in this study, including 25 patients with early-onset severe preeclampsia(EOPE) and 22 with late-onset severe preeclampsia (LOPE), with 25 women with normal pregnancy serving as control group.The antenatal blood and postpartum placenta were collected for immunohistochemical staining to detect PIBF expression inthe placenta and for testing serum PIBF level using ELISA. Flow cytometry was used to detect the percentage of circulatingTh1 and Th2 cells and the Th1/Th2 ratio was calculated. Results PIBF was expressed in decidual cells, syncytiotrophoblastsand partial cytotrophablasts. The serum PIBF levels were 213.58 ± 44.93 ng/ml in EOPE group, 243.00 ± 61.19 ng/ml in LOPEgroup and 273.91±48.57 ng/ml in control group. There were significant differences in serum PIBF, blood Th1/Th2 and placentaPIBF-IOD among the 3 groups (P<0.05). EOPE group had significantly lower serum PIBF, lower llacental PIBF quantity(PIBF-IOD) and higher blood Th1/Th2 than the control group (P<0.05). Serum PIBF in women with severe preeclampsia waspositively correlated with placenta PIBF-IOD and negatively with blood Th1/Th2 ratio (P<0.05), but a negative correlationbetween serum PIBF and 24-hour urinary protein was found only in EOPE group (P<0.05). Conclusion The immune toleranceimbalance mediated by PIBF may participate in the pathogenesis of severe preeclampsia. PIBF, the immune suppressorsecreted by lymphocytes of pregnancy women, is also a protective factor against severe preeclampsia, which is expected to bea new target in therapy.
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https://www.j-smu.com/EN/Y2015/V35/I06/848